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贺维顺, 刘爱华, 施立明. 1984: 苯和环磷酰胺诱发小鼠肝、骨髓和精原细胞染色体畸变的比较分析. 动物学研究, 5(2): 175-179.
引用本文: 贺维顺, 刘爱华, 施立明. 1984: 苯和环磷酰胺诱发小鼠肝、骨髓和精原细胞染色体畸变的比较分析. 动物学研究, 5(2): 175-179.
HE Wei-shun, LIU Ai-hua, SHI Li-ming. 1984. In vivo Induction of Chromosomal Aberration in Liver,Bone-Marrow and Spermatogonial Cells in Mice by Benzene and Cyclophosphamide. Zoological Research, 5(2): 175-179.
Citation: HE Wei-shun, LIU Ai-hua, SHI Li-ming. 1984. In vivo Induction of Chromosomal Aberration in Liver,Bone-Marrow and Spermatogonial Cells in Mice by Benzene and Cyclophosphamide. Zoological Research, 5(2): 175-179.

苯和环磷酰胺诱发小鼠肝、骨髓和精原细胞染色体畸变的比较分析

In vivo Induction of Chromosomal Aberration in Liver,Bone-Marrow and Spermatogonial Cells in Mice by Benzene and Cyclophosphamide

  • 摘要: 在同一个体小鼠上比较分析苯和环磷酰胺诱发的肝、骨髓和精原细胞的染色体畸变率。结果表明,这三种靶细胞的遗传毒理学敏感性是不同的。按每只0.01毫升的剂量皮下注射两次苯于部分肝切除的小鼠,按其诱发的染色体畸变率,敏感性的次序是肝>骨髓>精原细胞。而以环磷酰胺处理的小鼠(15微克/每克体重,腹腔注射),诱发的染色体畸变是骨髓>肝>精原细胞。苯和环磷酰胺诱发的染色体畸变类型无明显差别,主要都是染色单体型的畸变。这种在同一个体小鼠上比较分析三种靶细胞染色体畸变的方法,对于需要肝代谢活化的前致癌剂/前诱变剂活性的测定以及体内比较三种靶细胞的遗传毒性敏感性提供了新的检测途径。不同组织、器官对化学诱变剂敏感性的差异及其机制的研究,在遗传毒理学中是一项重要的研究课题。本文试图以苯和环磷酰胺作为检测剂,以同一个体上的肝、骨髓、精原细胞为靶细胞,比较分析诱发的染色体畸变率差异以期对遗传毒理学敏感性有较好的了解。

     

    Abstract: A highly dependable method for the detection of in vivo induction of chromosomal aberration has been developed in liver,bone-marrow and spermatogonial cells in mice subjected to partial hepatectomy.The inductivities of chromosomal aberrations by benzene and cyclophosphamide are different.When the partially hepatectomized mice were injected intraparitoneally with freshly prepared cyclophosphamide solution (15 μg/g body wt.),the inductivity to the three target cells is bone-marrow cells>regenerating liver cells>spermatogonial cells,whereas the inductivity of benzene (0.01 ml/mouse,2 subcutaneous injections) is regenerating liver cells>bone-marrow cells>spermatogonial cells.To develop this procedure will facilitate the detection of drug-induced clastogenic activity,particularly those requiring tissue-specific metabolic activated procarcinogens/promutagens and in vivo comparison of clastogenic sensitivity among the three types of tissues.

     

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